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Finding Patients At Risk for Rare Disease

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ThinkGenetic to Attend ACMG/SIMD Joint Meeting

March 10, 2023 by Ruth O'Keefe

ThinkGenetic announces its participation at the 2023 ACMG Annual Clinical Genetics Meeting which is being held in conjunction with the Society for Inherited Metabolic Disorders Meeting for the first time in Salt Lake City, Utah, this March.

News @SIMDtweets, #ACMGMtg23, #SIMD2023, ACMG, Annual Clinical Genetics Meeting, Dawn Laney, Jessica Dronen, medical genetics, metabolics, SIMD, Society for Inherited Metabolic Disorders

ThinkGenetic Announces Participation at 19th Annual WORLDSymposium™ 2023

February 8, 2023 by Ruth O'Keefe

ThinkGenetic announces that Chief Genetic Officer, Dawn Laney, MS, CGC, CCRC, will be participating in a 19th Annual WORLDSymposium™ Satellite Symposia entitled “Understanding Phenotypic Variability in Lysosomal Diseases – Gaining a Foothold in Precision Medicine” sponsored by Takeda Pharmaceutical Company Limited.

News Dawn Laney, lysosomal diseases, Takeda, Takeda Pharmaceutical Company Limited, WORLDSymposium

Extracting Electronic Health Record (EHR) Data Using Transfer Learning

January 9, 2023 by Corey Fournier, Senior Data Engineer

At ThinkGenetic, Inc. our goal is to reduce the time to diagnosis for genetic and rare conditions. Given they are rare, we must be cognizant of the time it takes […]

News, Technical Research algorithms, BERT model, clinical note, EHR, electronic health records, genetic conditino, genetic condition, Google, ICD-10, Medical Coding, medical record, misdiagnosed, Name Entity Recognition, Natural Language Processing, NLP, Procedures codes, Rare Disease, rare genetic disease, Relation Extraction, Semantic Role labeling, Shi and Lin, Snomed, structured data, T5, Text-to-text Transfer Transformers, undiagnosed, unstructured data

[Press Release] Guardian Research Network and ThinkGenetic Announce Collaborative Partnership to Accelerate Diagnosis and Treatment Options for Patients with Genetic Diseases and Inherited Predisposition to Cancer

July 28, 2022 by Ruth O'Keefe

 Guardian Research Network, Inc.® (GRN) and ThinkGenetic, Inc. announce a strategic collaboration to accelerate the diagnosis and support the development of treatment options for patients with rare and genetic diseases.

News, Press Releases algorithm, announcement, Bruce Braughton, Dave Jacob, diagnostic odyssey, digital health, EHR, electronic health records, genetic condition, genetic disease, GRN, Guardian Research Network, healthcare, Mark Watson, partnership, press release, PTC Therapeutics, Rare Disease, ThinkGenetic

Supporting Rare Disease Day 2022

February 25, 2022 by Jennifer Dykeman

February 28th is Rare Disease Day! In the United States, a disease is defined as rare if it affects less than 200,000 people. It is currently thought that there may be […]

Advocacy, Education, News advocacy, Find a Genetic Counselor, GARD, Genetic and Rare Disease Information Center, National Organization for Rare Diseases, National Society of Genetic Counselor, NIH, NORD, NSGC, patient services, Rare Disease Day

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Upcoming Events

Mar 10
March 10, 2026 - March 14, 2026

ACMG Annual Clinical Genetics Meeting 2026

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Together let’s systematically accelerate detecting at-risk  individuals.

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